Natural pseurotins inhibit proliferation and inflammatory responses through the inactivation of STAT signaling pathways in macrophages
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články
PubMed
32376338
DOI
10.1016/j.fct.2020.111348
PII: S0278-6915(20)30236-2
Knihovny.cz E-zdroje
- Klíčová slova
- Cytokines, Immunity, Macrophage, Natural pseurotin, Nitric oxide, STAT,
- MeSH
- cykliny metabolismus MeSH
- lipopolysacharidy farmakologie MeSH
- makrofágy účinky léků metabolismus MeSH
- mediátory zánětu metabolismus MeSH
- mitochondrie účinky léků metabolismus MeSH
- myši MeSH
- proliferace buněk účinky léků MeSH
- pyrrolidinony farmakologie MeSH
- RAW 264.7 buňky MeSH
- signální transdukce účinky léků MeSH
- transkripční faktor STAT3 metabolismus MeSH
- zánět prevence a kontrola MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- cykliny MeSH
- lipopolysacharidy MeSH
- mediátory zánětu MeSH
- pseurotin MeSH Prohlížeč
- pyrrolidinony MeSH
- Stat3 protein, mouse MeSH Prohlížeč
- transkripční faktor STAT3 MeSH
BACKGROUND: Natural pseurotins, secondary metabolites of fungi, commonly produced by various species such as Aspergillus flavus with suggested significant biological effects. However, little is known about effects of pseurotins on immune system functions. METHODS: Effects of pseurotin A and D on proliferation and viability of macrophage RAW 264.7 cells were evaluated together with mitochondrial respiration and glycolysis. Macrophage response to lipopolysaccharide was analyzed based on determination of nitric oxide (NO) production, expression of inducible NO synthase (iNOS), interleukin 6 (IL-6) and tumor necrosis factor production. Activation of selected signaling pathways, particularly STAT and MAPK, as well as expression of cyclins were determined. RESULTS: Natural pseurotins A and D in concentrations of up to 50 μM significantly inhibit proliferation of RAW 264.7 macrophages which was not complemented by induction of cell toxicity. The inhibition of cell proliferation was accompanied by downregulation of expression of cyclins and mitochondrial respiration via inhibition of particularly STAT3 phosphorylation. Both pseurotins significantly inhibited production of NO, expression of iNOS and IL-6 production. CONCLUSION: Our results advance the current mechanistic understanding of the pseurotin-induced inhibition of proliferation, metabolic respiration and functional responses in macrophages by linking the effect to JAK/STAT signaling pathway.
Citace poskytuje Crossref.org
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